Mitochondrial complex III deficiency, nuclear type 11

Preferred Label : Mitochondrial complex III deficiency, nuclear type 11;

Symbol : MC3DN11;

Type : Phenotype, molecular basis known;

Prefixed ID : #620137;

Details

Origin ID

620137;

UMLS CUI

C5774259;

Genes related to phenotype
- Ubiquinol-cytochrome C reductase hinge protein [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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